Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11714557	0.91[ASN][1000 genomes]
rs11924192	0.88[ASN][1000 genomes]
rs12632055	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13314516	0.81[ASN][1000 genomes]
rs1447695	0.86[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1447696	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1447699	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1562483	0.90[ASN][1000 genomes]
rs16841959	0.91[ASN][1000 genomes]
rs1868166	0.84[ASN][1000 genomes]
rs2400300	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67368005	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6774239	0.88[ASN][1000 genomes]
rs6802542	0.92[ASN][1000 genomes]
rs73222791	0.91[ASN][1000 genomes]
rs73222793	0.91[ASN][1000 genomes]
rs73225024	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7428606	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7619098	0.82[ASN][1000 genomes]
rs9850495	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877515	chr3:134460368-134591138	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134459600-134460400	Enhancers	HSMMtube	muscle
2	chr3:134459600-134460800	Enhancers	Fetal Muscle Leg	muscle

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